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临床试验/JPRN-UMIN000000541
JPRN-UMIN000000541已完成未知

The study on the efficacy and safety of pharmacokinetics of mycophenolate mofetil for pediatric renal transplantation - Mycophenolate mofetil for pediatric renal transplantation

Japanese Study group of Pediatric Renal Transplantation0 个研究点目标入组 50 人开始时间: 2007年1月5日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
ot applicable 至 20years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1. The acute rejection after renal transplantation. 2. Use ofimmunosuppressant which works the same way as MMF does. 3. Prior exposure to live vaccine within one month before the treatment of MMF 4. Active peptic ulcer disease 5. Severe liver dysfunction 6. Leucopenia at study entry 7. Active systemic infection 8. Malignancy 9. Hemorrhagic diathesis 10. Refractory diarrhea 11. Medical history of severe allergy or drug hypersensitivity 12. ABO-incompatible kidney allograft 13. Anti-donor antibody positive patients 14. Pregnancy 15. Judged inappropriate for this study by the physicians

研究者

发起方
Japanese Study group of Pediatric Renal Transplantation

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